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利用反义寡核苷酸在 PC12 神经元分化过程中对 NF1 外显子 23a 的可变剪接进行生理调节。

Using antisense oligonucleotides for the physiological modulation of the alternative splicing of NF1 exon 23a during PC12 neuronal differentiation.

机构信息

Hereditary Cancer Group, Germans Trias i Pujol Research Institute (IGTP), Can Ruti Biomedical Campus, Badalona, Barcelona, Spain.

Institute for Research in Biomedicine (IRB Barcelona), Parc Cientific de Barcelona, Barcelona, Spain.

出版信息

Sci Rep. 2021 Feb 11;11(1):3661. doi: 10.1038/s41598-021-83152-w.

Abstract

Neurofibromatosis Type 1 (NF1) is a genetic condition affecting approximately 1:3500 persons worldwide. The NF1 gene codes for neurofibromin protein, a GTPase activating protein (GAP) and a negative regulator of RAS. The NF1 gene undergoes alternative splicing of exon 23a (E23a) that codes for 21 amino acids placed at the center of the GAP related domain (GRD). E23a-containing type II neurofibromin exhibits a weaker Ras-GAP activity compared to E23a-less type I isoform. Exon E23a has been related with the cognitive impairment present in NF1 individuals. We designed antisense Phosphorodiamidate Morpholino Oligomers (PMOs) to modulate E23a alternative splicing at physiological conditions of gene expression and tested their impact during PC12 cell line neuronal differentiation. Results show that any dynamic modification of the natural ratio between type I and type II isoforms disturbed neuronal differentiation, altering the proper formation of neurites and deregulating both the MAPK/ERK and cAMP/PKA signaling pathways. Our results suggest an opposite regulation of these pathways by neurofibromin and the possible existence of a feedback loop sensing neurofibromin-related signaling. The present work illustrates the utility of PMOs to study alternative splicing that could be applied to other alternatively spliced genes in vitro and in vivo.

摘要

神经纤维瘤病 1 型(NF1)是一种影响全球约 1:3500 人的遗传疾病。NF1 基因编码神经纤维瘤蛋白,一种 GTP 酶激活蛋白(GAP)和 RAS 的负调节剂。NF1 基因通过外显子 23a(E23a)的选择性剪接,编码位于 GAP 相关结构域(GRD)中心的 21 个氨基酸。与缺乏 E23a 的 I 型同工型相比,含有 E23a 的 II 型神经纤维瘤蛋白表现出较弱的 Ras-GAP 活性。E23a 外显子与 NF1 个体中存在的认知障碍有关。我们设计了反义磷酸二酰胺吗啉代寡聚物(PMO)来调节生理条件下基因表达的 E23a 选择性剪接,并在 PC12 细胞系神经元分化过程中测试了它们的影响。结果表明,I 型和 II 型同工型之间天然比例的任何动态改变都会干扰神经元分化,改变神经突的正确形成,并使 MAPK/ERK 和 cAMP/PKA 信号通路失调。我们的结果表明,神经纤维瘤蛋白对这些途径的调节作用相反,并且可能存在一种反馈回路来感知神经纤维瘤蛋白相关的信号。本工作说明了 PMO 用于研究选择性剪接的实用性,该方法可应用于体外和体内的其他选择性剪接基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec80/7878752/769ade9975d3/41598_2021_83152_Fig1_HTML.jpg

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